FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EVERCROSS 0.035 OTW PTA DILATION CATHETER

K Number: K103322 · Decision Dec 6, 2010
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
402
Applicant Total
35
Review Days
24

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Basic Information

Device Name
EVERCROSS 0.035 OTW PTA DILATION CATHETER
K Number
K103322
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ev3, Inc.
Date Received
November 12, 2010
Decision Date
December 6, 2010
Product Code
LIT
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LIT Catheter, Angioplasty, Peripheral, Transluminal

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Other Clearances by Ev3, Inc.

K Number Device Name
K141118 NANOCROSS EITE 0.014 OVER-THE-WIRE PTA BALLOON DILATATION CATHETER
K132777 NANOCROSS ELITE .14 OVER-THE-WIRE PTA, BALLOON DILATION CATHETER
K130911 RAPIDCROSS PTA RAPID EXCHANGE BALLOON DILATATION CATHETER
K123544 RAPIDCROSS PTA RAPID EXCHANGE, BALLOON DILATATION CATHETER
K111723 TURBOHAWK PERIPHERAL PLAQUE EXCISION SYSTEM
K111010 SPIDERFX EMBOLIC PROTECTION DEVICE
K111490 MARKSMAN CATHETER, *REFERS TO DIFFERENT CATHETER WORKING LENGHTS, DISTAL SINGLE COILED LENGTHS AND DISTAL SHAFT LENGTHS
K110319 EVERCROSS 0.035 OTW PTA DILATATION CATHETER
K103618 TURBOHAWK PEROPHERAL PLAQUE EXCISION SYSTEM
K100063 HYPERFORM OCCLUSION BALLOON CATHETER, HYPERGLIDE OCCLUSION BALLOON CATHETER, HYPERGLIDE OCCLUSION BALLOON CATHETER MODEL
Search all 35 clearances from Ev3, Inc. →